Variant report

Variant	esv1838483
Chromosome Location	chr16:81061827-81070110
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:694)
CpG islands
(count:489)
Chromatin interactive
region (count:43)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:694 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr16:81069098-81069480	HepG2	liver:	n/a	n/a
2	ARID3A	chr16:81069192-81069429	K562	blood:	n/a	n/a
3	ATF3	chr16:81069273-81069432	GM12878	blood:	n/a	n/a
4	ATF3	chr16:81069117-81069467	K562	blood:	n/a	n/a
5	ATF3	chr16:81069206-81069438	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr16:81069088-81069501	GM12878	blood:	n/a	n/a
7	BACH1	chr16:81070075-81070126	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr16:81068962-81069496	A549	lung:	n/a	n/a
9	BCLAF1	chr16:81069039-81069544	GM12878	blood:	n/a	n/a
10	BCLAF1	chr16:81069567-81070166	GM12878	blood:	n/a	chr16:81069865-81069878 chr16:81069919-81069932 chr16:81069914-81069927 chr16:81069981-81069994
11	BHLHE40	chr16:81069849-81070026	GM12878	blood:	n/a	chr16:81069922-81069938 chr16:81069905-81069921 chr16:81069916-81069932
12	BHLHE40	chr16:81069151-81069458	K562	blood:	n/a	n/a
13	BHLHE40	chr16:81069115-81069527	GM12878	blood:	n/a	n/a
14	BHLHE40	chr16:81070063-81070082	K562	blood:	n/a	n/a
15	BRCA1	chr16:81069328-81069382	GM12878	blood:	n/a	n/a
16	BRCA1	chr16:81069301-81069328	HepG2	liver:	n/a	n/a
17	BRCA1	chr16:81070020-81070047	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr16:81069139-81069434	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr16:81069189-81069476	H1-hESC	embryonic stem cell:	n/a	n/a
20	CBX3	chr16:81069029-81069463	K562	blood:	n/a	n/a
21	CCNT2	chr16:81069068-81070115	K562	blood:	n/a	n/a
22	CEBPB	chr16:81069045-81069493	Hela-S3	cervix:	n/a	chr16:81069173-81069184
23	CEBPB	chr16:81069788-81070933	Hela-S3	cervix:	n/a	chr16:81070188-81070199 chr16:81070187-81070198
24	CEBPB	chr16:81069093-81069426	H1-hESC	embryonic stem cell:	n/a	chr16:81069173-81069184
25	CEBPB	chr16:81070006-81070438	K562	blood:	n/a	chr16:81070188-81070199 chr16:81070187-81070198
26	CEBPB	chr16:81068907-81069337	GM12878	blood:	n/a	chr16:81069173-81069184
27	CEBPB	chr16:81070047-81070338	HepG2	liver:	n/a	chr16:81070188-81070199 chr16:81070187-81070198
28	CEBPB	chr16:81069945-81070447	MCF-7	breast:	n/a	chr16:81070188-81070199 chr16:81070187-81070198
29	CEBPB	chr16:81069118-81069302	HepG2	liver:	n/a	chr16:81069173-81069184
30	CEBPB	chr16:81070001-81070214	H1-hESC	embryonic stem cell:	n/a	chr16:81070188-81070199 chr16:81070187-81070198
31	CEBPB	chr16:81070098-81070372	A549	lung:	n/a	chr16:81070188-81070199 chr16:81070187-81070198
32	CEBPB	chr16:81070008-81071044	K562	blood:	n/a	chr16:81070188-81070199 chr16:81070187-81070198
33	CEBPB	chr16:81070014-81070377	IMR90	lung:	n/a	chr16:81070188-81070199 chr16:81070187-81070198
34	CEBPB	chr16:81069920-81070447	A549	lung:	n/a	chr16:81070188-81070199 chr16:81070187-81070198
35	CEBPD	chr16:81069215-81069605	HepG2	liver:	n/a	n/a
36	CEBPZ	chr16:81069145-81069345	HepG2	liver:	n/a	n/a
37	CHD1	chr16:81069681-81070304	H1-hESC	embryonic stem cell:	n/a	chr16:81070007-81070017
38	CHD1	chr16:81069264-81070073	GM12878	blood:	n/a	chr16:81070007-81070017 chr16:81069401-81069411
39	CHD2	chr16:81069869-81070032	K562	blood:	n/a	chr16:81070007-81070017
40	CHD2	chr16:81069194-81069546	Hela-S3	cervix:	n/a	chr16:81069401-81069411
41	CHD2	chr16:81069822-81070226	Hela-S3	cervix:	n/a	chr16:81070007-81070017
42	CHD2	chr16:81069962-81070226	H1-hESC	embryonic stem cell:	n/a	chr16:81070007-81070017
43	CHD2	chr16:81069223-81069507	GM12878	blood:	n/a	chr16:81069401-81069411
44	CHD2	chr16:81069169-81069394	K562	blood:	n/a	n/a
45	CHD2	chr16:81069302-81069353	HepG2	liver:	n/a	n/a
46	CHD2	chr16:81069113-81069460	H1-hESC	embryonic stem cell:	n/a	chr16:81069401-81069411
47	CREB1	chr16:81069193-81069599	A549	lung:	n/a	n/a
48	CREB1	chr16:81069234-81069501	A549	lung:	n/a	n/a
49	CREB1	chr16:81069130-81069569	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr16:81069200-81069350	GM06990	blood:	n/a	chr16:81069291-81069307 chr16:81069272-81069280

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr16:81069742-81069792	HNPCEpiC	eye:	n/a
2	chr16:81069742-81069792	HNPCEpiC	eye:	n/a
3	chr16:81069184-81069234	SK-N-SH_RA	brain:	n/a
4	chr16:81069244-81069294	NB4	blood:	n/a
5	chr16:81069293-81069343	GM12892	blood:	n/a
6	chr16:81066575-81066625	HepG2	liver:	n/a
7	chr16:81069742-81069792	NB4	blood:	n/a
8	chr16:81066575-81066625	AG04450	lung:	fetal
9	chr16:81069742-81069792	SK-N-SH	brain:	n/a
10	chr16:81069742-81069792	HRPEpiC	eye:	n/a
11	chr16:81069748-81069798	AG04449	skin:	fetal
12	chr16:81069293-81069343	RPTEC	kidney:	n/a
13	chr16:81069748-81069798	SKMC	muscle:	n/a
14	chr16:81069742-81069792	AG04449	skin:	fetal
15	chr16:81069748-81069798	NHBE	bronchial:	n/a
16	chr16:81069293-81069343	HepG2	liver:	n/a
17	chr16:81066575-81066625	Caco-2	colon:	n/a
18	chr16:81069748-81069798	AoSMC	blood vessel:	n/a
19	chr16:81069005-81069055	HepG2	liver:	n/a
20	chr16:81069742-81069792	ovcar-3	ovarian:	n/a
21	chr16:81069748-81069798	PrEC	prostate:	n/a
22	chr16:81069005-81069055	HRCEpiC	kidney:	n/a
23	chr16:81069740-81069790	AG10803	skin:	n/a
24	chr16:81066575-81066625	ProgFib	skin:	n/a
25	chr16:81069005-81069055	PrEC	prostate:	n/a
26	chr16:81069005-81069055	HEEpiC	esophagus:	n/a
27	chr16:81069184-81069234	K562	blood:	n/a
28	chr16:81069005-81069055	AG04450	lung:	fetal
29	chr16:81069742-81069792	AG09319	gingival:	n/a
30	chr16:81069005-81069055	K562	blood:	n/a
31	chr16:81069005-81069055	HRPEpiC	eye:	n/a
32	chr16:81069293-81069343	NHDF-neo	bronchial:	n/a
33	chr16:81069742-81069792	PrEC	prostate:	n/a
34	chr16:81069293-81069343	HCT-116	colon:	n/a
35	chr16:81069740-81069790	AoSMC	blood vessel:	n/a
36	chr16:81069748-81069798	LNCaP	prostate:	n/a
37	chr16:81069742-81069792	PANC-1	pancreas:	n/a
38	chr16:81069184-81069234	IMR90	lung:	fetal
39	chr16:81069740-81069790	SK-N-SH	brain:	n/a
40	chr16:81069740-81069790	NHBE	bronchial:	n/a
41	chr16:81069742-81069792	CMK	blood:	n/a
42	chr16:81069748-81069798	U87	brain:	n/a
43	chr16:81069293-81069343	HPAEpiC	pulmonary alveolar:	n/a
44	chr16:81069740-81069790	HEEpiC	esophagus:	n/a
45	chr16:81069244-81069294	ECC-1	luminal epithelium:	n/a
46	chr16:81069005-81069055	GM12891	blood:	n/a
47	chr16:81069742-81069792	K562	blood:	n/a
48	chr16:81069184-81069234	PrEC	prostate:	n/a
49	chr16:81069293-81069343	HMEC	breast:	n/a
50	chr16:81069244-81069294	NHDF-neo	bronchial:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr16:81039925..81040655-chr16:81068862..81069785,3	MCF-7	breast:
2	chr16:81056423..81058180-chr16:81069392..81072113,2	MCF-7	breast:
3	chr16:81067878..81071089-chr16:81109086..81112093,6	K562	blood:
4	chr16:81053262..81055946-chr16:81062478..81064809,2	K562	blood:
5	chr16:81038105..81044923-chr16:81066300..81070952,14	MCF-7	breast:
6	chr16:81037996..81043724-chr16:81066407..81071400,11	MCF-7	breast:
7	chr16:81067084..81072191-chr16:81106033..81112629,21	MCF-7	breast:
8	chr16:81061192..81062937-chr16:81110399..81112342,2	MCF-7	breast:
9	chr16:81062101..81064821-chr16:81128185..81130104,2	MCF-7	breast:
10	chr16:81043779..81046119-chr16:81060874..81062593,2	MCF-7	breast:
11	chr16:81068163..81070898-chr16:81108747..81112001,7	MCF-7	breast:
12	chr16:81068976..81069841-chr16:81110418..81110934,2	MCF-7	breast:
13	chr16:81055761..81058462-chr16:81067542..81069697,2	K562	blood:
14	chr16:81068890..81071040-chr16:81770218..81773249,4	MCF-7	breast:
15	chr16:81068964..81069731-chr16:81231614..81232947,4	MCF-7	breast:
16	chr16:81051240..81053871-chr16:81067800..81070435,3	K562	blood:
17	chr16:81054446..81058037-chr16:81066516..81068816,3	MCF-7	breast:
18	chr16:81068173..81071730-chr16:81126382..81131671,6	MCF-7	breast:
19	chr16:81037151..81044642-chr16:81065528..81070966,16	K562	blood:
20	chr16:81069280..81069978-chr21:48054904..48055633,2	Hela-S3	cervix:
21	chr16:81069108..81070906-chr16:81231938..81234335,3	MCF-7	breast:
22	chr16:81037151..81042784-chr16:81066438..81073797,14	K562	blood:
23	chr16:81052685..81055352-chr16:81069386..81070952,2	MCF-7	breast:
24	chr16:81068545..81070466-chr16:81128738..81130368,2	K562	blood:
25	chr16:81056962..81059865-chr16:81068197..81070898,3	K562	blood:
26	chr16:81066967..81071215-chr16:81128766..81132498,3	MCF-7	breast:
27	chr16:81060980..81065115-chr16:81066790..81068667,3	K562	blood:
28	chr16:81067728..81071580-chr16:81109086..81113987,13	K562	blood:
29	chr16:81067967..81070895-chr16:81477501..81479169,2	K562	blood:
30	chr16:81061882..81066764-chr16:81067446..81071538,9	MCF-7	breast:
31	chr16:81052555..81056532-chr16:81060352..81063207,4	K562	blood:
32	chr16:81068207..81071925-chr16:81073357..81079831,13	MCF-7	breast:
33	chr16:81068545..81070561-chr16:81128158..81130238,2	K562	blood:
34	chr16:81068843..81069464-chr16:81129450..81130206,2	MCF-7	breast:
35	chr16:81069337..81069924-chr17:39845078..39845594,2	Hela-S3	cervix:
36	chr16:81069322..81070029-chr5:112256640..112257405,2	Hela-S3	cervix:
37	chr16:81065817..81067456-chr16:81067687..81069877,2	K562	blood:
38	chr16:81066324..81068444-chr16:81068507..81070080,2	MCF-7	breast:
39	chr16:81061882..81066764-chr16:81067446..81071538,9	MCF-7	breast:
40	chr16:81069395..81071569-chr16:81120451..81122846,2	K562	blood:
41	chr16:81043453..81045106-chr16:81060725..81063706,2	MCF-7	breast:
42	chr16:81068894..81069816-chr16:81231960..81232923,14	MCF-7	breast:
43	chr16:81041193..81042878-chr16:81061332..81063223,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C16orf61-1	chr16:81069274-81069339	ENSG00000260213.1
2	lnc-C16orf61-1	chr16:81068360-81068531	ENSG00000260213.1
3	lnc-C16orf61-1	chr16:81068360-81068453	NONHSAT143927
4	lnc-C16orf61-1	chr16:81068360-81068531	ENSG00000260213.1
5	lnc-ATMIN-1	chr16:81064375-81065090	ENSG00000261061.1
6	lnc-C16orf61-1	chr16:81069274-81069364	ENSG00000260213.1

No data

Variant related genes	Relation type
ATMIN	TF binding region
ENSG00000261061	TF binding region
ENSG00000260213	TF binding region
ATMIN	CpG island
ENSG00000261061	CpG island
ENSG00000260213	CpG island
ENSG00000140905	chromatin interactions
ENSG00000166454	chromatin interactions
ENSG00000261061	chromatin interactions
ENSG00000173812	chromatin interactions
ENSG00000166473	chromatin interactions
ENSG00000261218	chromatin interactions
ENSG00000103121	chromatin interactions
ENSG00000260643	chromatin interactions
ENSG00000245059	chromatin interactions
ENSG00000260213	chromatin interactions
ENSG00000153815	chromatin interactions
ENSG00000129625	chromatin interactions
ENSG00000197943	chromatin interactions
ENSG00000160310	chromatin interactions
ENSG00000166455	chromatin interactions
ENSG00000166451	chromatin interactions

Extended variants
information (count: 373 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:373 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2549887	chr16:81061827-81061828	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs369053141	chr16:81061910-81061911	Strong transcription Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs201010198	chr16:81061923-81061924	Strong transcription Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs371708815	chr16:81061924-81061925	Strong transcription Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs528276216	chr16:81061994-81061995	Strong transcription Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs2549888	chr16:81062030-81062031	Strong transcription Weak transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs147282961	chr16:81062040-81062041	Strong transcription Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs13331094	chr16:81062108-81062109	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs368203064	chr16:81062152-81062153	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs534014143	chr16:81062153-81062154	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs373653193	chr16:81062155-81062156	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs114305409	chr16:81062157-81062158	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs200783827	chr16:81062164-81062165	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs71376378	chr16:81062171-81062172	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs368796896	chr16:81062175-81062176	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs537518607	chr16:81062191-81062192	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs370171009	chr16:81062214-81062215	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs373383356	chr16:81062230-81062231	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs377398346	chr16:81062259-81062260	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs201073061	chr16:81062263-81062264	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs71400134	chr16:81062264-81062265	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs370635113	chr16:81062290-81062291	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs370371110	chr16:81062302-81062303	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs374449585	chr16:81062307-81062308	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs184980265	chr16:81062339-81062340	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs35552248	chr16:81062362-81062363	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs575031262	chr16:81062449-81062450	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs139018356	chr16:81062478-81062479	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs146994969	chr16:81062489-81062490	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs563261288	chr16:81062519-81062520	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs530412757	chr16:81062544-81062545	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs189444666	chr16:81062569-81062570	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs73595485	chr16:81062573-81062574	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs180956450	chr16:81062716-81062717	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs185768959	chr16:81062747-81062748	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs117167180	chr16:81062791-81062792	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs542693603	chr16:81062840-81062841	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs548305052	chr16:81062846-81062847	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs570066534	chr16:81062881-81062882	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs114145162	chr16:81062883-81062884	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs189640488	chr16:81062909-81062910	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs570601078	chr16:81062948-81062949	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs371477846	chr16:81062978-81062979	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs534894072	chr16:81063006-81063007	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs181901938	chr16:81063012-81063013	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs186195469	chr16:81063056-81063057	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs2602429	chr16:81063149-81063150	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs557352256	chr16:81063152-81063153	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs575249897	chr16:81063165-81063166	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs536506124	chr16:81063172-81063173	Strong transcription Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16702952	CNVD
Medulloblastoma	16968546	CNVD
Prostate cancer	19242612	CNVD
Cancer	22429812	CNVD
Ewing''s sarcoma	21437220	CNVD
Ewing''s sarcoma	22429812	CNVD
Melanoma	18172304	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Multiple myeloma	21628407	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17001317	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17603634	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	17245344	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	18438408	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Autism	21865298	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	CNVD
Neuroblastoma	18923524	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Obesity	20622171	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	22228453	CNVD

Chromatin state (count:445 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:81041800-81069000	Weak transcription	Ovary	ovary
2	chr16:81041800-81069000	Weak transcription	Small Intestine	intestine
3	chr16:81042000-81069000	Weak transcription	Esophagus	oesophagus
4	chr16:81042000-81069000	Weak transcription	Pancreas	Pancrea
5	chr16:81042000-81069600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr16:81042200-81068800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr16:81042200-81069000	Weak transcription	Colonic Mucosa	Colon
8	chr16:81042200-81069600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr16:81042400-81069000	Weak transcription	Brain Germinal Matrix	brain
10	chr16:81042400-81069000	Weak transcription	Fetal Heart	heart
11	chr16:81042600-81064200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr16:81043000-81063800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr16:81043000-81064600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr16:81043000-81065400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
15	chr16:81043200-81062800	Strong transcription	K562	blood
16	chr16:81043200-81065200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
17	chr16:81044000-81064400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr16:81044000-81065200	Strong transcription	Thymus	Thymus
19	chr16:81044400-81064000	Strong transcription	HUES64 Cell Line	embryonic stem cell
20	chr16:81044600-81064000	Strong transcription	H1 Cell Line	embryonic stem cell
21	chr16:81044800-81065200	Strong transcription	Hela-S3	cervix
22	chr16:81045000-81064000	Strong transcription	Dnd41	blood
23	chr16:81045200-81062800	Strong transcription	Osteobl	bone
24	chr16:81045200-81065200	Strong transcription	A549	lung
25	chr16:81045400-81065200	Strong transcription	HUES48 Cell Line	embryonic stem cell
26	chr16:81046400-81064600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr16:81047800-81069000	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr16:81048400-81069000	Weak transcription	Fetal Kidney	kidney
29	chr16:81048600-81069000	Weak transcription	Fetal Brain Female	brain
30	chr16:81049000-81069000	Weak transcription	Right Ventricle	heart
31	chr16:81050200-81069000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
32	chr16:81050600-81069000	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr16:81053000-81069400	Weak transcription	Aorta	Aorta
34	chr16:81053400-81064800	Weak transcription	Primary T helper cells PMA-I stimulated	--
35	chr16:81053400-81068800	Weak transcription	Brain Angular Gyrus	brain
36	chr16:81053600-81069000	Weak transcription	Brain Anterior Caudate	brain
37	chr16:81053800-81068800	Weak transcription	Brain Cingulate Gyrus	brain
38	chr16:81054000-81068800	Weak transcription	Brain Substantia Nigra	brain
39	chr16:81054200-81064800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr16:81054200-81069000	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr16:81055200-81063200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr16:81055200-81068800	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr16:81055200-81069400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr16:81055200-81069600	Weak transcription	Spleen	Spleen
45	chr16:81055400-81069000	Weak transcription	Primary T cells fromperipheralblood	blood
46	chr16:81055400-81069200	Weak transcription	NHLF	lung
47	chr16:81055600-81069000	Weak transcription	Lung	lung
48	chr16:81055600-81069400	Weak transcription	Gastric	stomach
49	chr16:81055600-81069600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr16:81055800-81069000	Weak transcription	Rectal Mucosa Donor 29	rectum

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